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Benzoylcyclohexane on irradiation on a dry silica gel surface, undergo an oxidative cleavage to give adipic acid and subsituted benzoic acid along with the Norrish Type II product. The kinetics of racemization of benzoylcyclohexane (2-benzoylcyclohexanone) in hexane, ethanol and their mixtures has been investigated by time dependence of enantiomeric purity using enantioselective HPLCIt was used to investigate the crosslinked cyclohexyl phenyl compounds under thermal and aquathermal conditions. It was used to examine the effects of molecular changes in the benzophenone molecule on phototoxic behavior. Benzoylcyclohexane on irradiation on a dry silica gel surface, undergo an oxidative cleavage to give adipic acid and subsituted benzoic acid along with the Norrish Type II product. The kinetics of racemization of benzoylcyclohexane (2-benzoylcyclohexanone) in hexane, ethanol and their mixtures has been investigated by time dependence of enantiomeric purity using enantioselective HPLC It was used to investigate the crosslinked cyclohexyl phenyl compounds under thermal and aquathermal conditions. It was used to examine the effects of molecular changes in the benzophenone molecule on phototoxic behavior.
中文名称
环己基苯基酮
英文名称
Cyclohexyl Phenyl Ketone
中文别名
环己基苯基甲酮 | 苯甲酰环己烷
英文别名
Benzoyl cyclohexane | cyclohexyl(phenyl);methanone | DTXSID5048182 | Cyclohexyl(phenyl)methanone # | 0NU53987V8 | Z104477736 | Cyclohexyl phenyl ketone | BRN 2046712 | Cyclohexyl(phenyl)methanone | MFCD00001467 | FT-0624211 | NCGC00257313-01 | InChI=1/C13
CAS号
712-50-5
分子式
C13H16O
分子量
188.27 g/mol
精确质量
≥98%(GC)
PSA
17.100 Ų
Logp
3.700
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标准品/环己基苯基酮 ≥98.0% 100mg

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